Haemophilia
短名 | Haemophilia. |
Journal Impact | 2.87 |
国际分区 | HEMATOLOGY(Q2) |
期刊索引 | SCI Q2中科院 2 区 |
ISSN | 1351-8216, 1365-2516 |
h-index | 104 |
国内分区 | 医学(2区)医学血液学(3区) |
HAEMOPHILIA 是一本国际期刊,致力于交流有关血友病综合护理的信息。该杂志包含与血友病护理相关的评论文章、原始科学论文和病例报告,并经常补充。涵盖的主题包括:遗传性和获得性凝血因子缺乏症:血友病 A、B、VON WILLEBRAND 病、因子 V、VII、X 和 XI 的缺乏 凝血因子缺乏症的替代疗法 发展中国家输血传播疾病的成分治疗 血友病护理和儿科,骨科、妇产科护理实验室诊断携带者检测心理社会关注经济问题审计遗传性血小板疾病。
期刊主页投稿网址涉及主题 | 医学生物遗传学外科儿科内科学血友病血友病A病理化学免疫学生物化学心理学精神科 |
出版信息 | 出版商: John Wiley and Sons Inc,出版周期: Quarterly,期刊类型: journal |
基本数据 | 创刊年份: 1995,原创研究文献占比: 86.21%,自引率:23.30%, Gold OA占比: 36.29% |
平均审稿周期 | 网友分享经验:一般,3-6周 |
平均录用比例 | 网友分享经验:较易 |
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最新文章
Development of the coreHEM mental health patient‐reported outcome measure – A novel mental health outlook measure for people with haemophilia
2024-9-5
Determination of body composition by dual x‐ray absorptiometry in persons with haemophilia
2024-9-1
Issue Information
2024-9-1
Differences and similarities in patient‐reported outcomes among men and women with haemophilia
2024-8-27
Comprehensive laboratory assessment of lonoctocog alfa versus octocog alfa in severe haemophilia A
2024-8-20
Driving improvement of diagnosis and awareness of heavy menstrual bleeding in women among physicians
2024-8-20
Transitioning patients with severe haemophilia A from emicizumab prophylaxis to valoctocogene roxaparvovec gene therapy: Real‐world clinical experience
2024-8-13
Factor V haemostatic diathesis impairing thrombin activation, membrane binding and circulating antigen level due to a novel compound heterozygous mutation, Leu1821Ser and Gly2192Cys
2024-8-8
Bioclinical features of haemophilia patients in Benin in 2023: Towards better care
2024-8-8
Sexual functioning in men with haemophilia: Data from the haemophilia in the Netherlands‐6 study
2024-8-7
Acute neuromuscular and perceptual responses to blood flow restriction exercise in adults with severe haemophilia: A pilot study
2024-8-4
Diagnosis and management of factor XI alloinhibitors in patients with congenital factor XI deficiency—A large single‐centre experience
2024-7-22
Multiyear, real‐world, retrospective cohort study using a patient‐centric approach to evaluate the burden of haemophilia B in the United States
2024-7-22
Application of the PECARN head trauma rule to patients with haemophilia in the paediatric emergency department: A 15‐year retrospective study
2024-7-21
Review of interventions and effectiveness for heavy menstrual bleeding in women with moderate and severe von Willebrand disease
2024-7-21
Efficacy of a 1:1 ratio VWF/FVIII concentrate in patients with von Willebrand disease
2024-7-15
Moving towards Normalization of haemostasis and health equity: Evolving treatment goals for haemophilia A
2024-7-10
A clinical practice guideline for primary care physiotherapy in patients with haemophilia
2024-7-10
Recombinant FVIII replacement products for haemophilia A: An updated valuation by indirect comparison measuring area under the curve
2024-7-9
Valoctocogene roxaparvovec gene therapy provides durable haemostatic control for up to 7 years for haemophilia A
2024-7-8
Issue Information
2024-7-1
Real world management of individuals with severe FXI deficiency and its impact on clinical outcomes: Experience from a haemophilia treatment centre
2024-7-1
Acquired haemophilia A in Finland: A nationwide study of incidence, treatment and outcomes
2024-6-28
Minimal interference of concizumab with standard clinical coagulation laboratory assays – An in vitro study
2024-6-25
A qualitative study on the perioperative experiences and demands of haemophilic arthropathy patients undergoing total joint replacement
2024-6-24
Emicizumab plasma levels after accelerated saturation in acquired haemophilia A
2024-6-24
Identifying hemophilia B carriers: Utility of aPTT, factor IX levels and ratios of factor IX to other Vitamin K dependent factors
2024-6-24
Accuracy and clinical role of digital templating for total knee arthroplasty performed on haemophilic knees
2024-6-20
Real‐world experience of rIX‐FP prophylaxis at dosing intervals of 14 days or more in adult patients with haemophilia B in Italy – Results from IDEAL Part B
2024-6-20
A case of bruising and joint hypermobility: The need to consider genetic testing for platelet disorders
2024-6-16
Reduced doses of emicizumab achieve good efficacy: Results from a national‐wide multicentre real‐world study in China
2024-6-9
Comparison of the kinematic analysis of indoor and outdoor gait in people with haemophilia and total knee replacement
2024-6-9
Evaluation of one‐stage and chromogenic assays for the laboratory measurement of factor VIII activity following valoctocogene roxaparvovec infusion
2024-6-6
Effects of resistance training on muscle strength in adults with haemophilia: A systematic review and meta‐analysis
2024-6-6
Low bleeding rates after intramuscular Covid‐19 vaccination in patients with haemophilia and von Willebrand disease: Outcome data from the Swedish haemophilia registry
2024-6-6
Functional clinical motor performance tests to assess potential fall risks in patients with haemophilia: A case‐control study
2024-6-4
Humanistic burden of haemophilia A without inhibitors: A cross‐sectional analysis of the HemoLIFE study
2024-6-2
Oral surgery in people with inherited bleeding disorder: A retrospective study
2024-6-2
Self‐conducted sonographic monitoring of the knee in patients with haemophilia—A feasibility study
2024-6-2
Limited value of testing for factor XIII and α2‐antiplasmin deficiency in patients with a bleeding disorder of unknown cause
2024-5-29
The relevance of MRI findings in joints of persons with haemophilia: Insights from the last decade
2024-5-29
Association between cognitive impairment and functional limitations in everyday life in patients with haemophilia in Hong Kong
2024-5-28
Treatment of thrombotic cardiovascular diseases in people with haemophilia: A Japanese consensus study
2024-5-23
Inherited coagulation factor VII deficiency in Taiwan: Two novel <i>F7</i> variants with relevant regional features in 33 patients
2024-5-23
Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease
2024-5-23
Heterozygous large deletion mimicking homozygous substitution in <i>MCFD2</i> in a patient with combined Factor V and Factor VIII deficiency
2024-5-19
Retrospective chart review of GI bleeding in people with von Willebrand disease
2024-5-15
Spectrum, clinical characteristics and outcome of von Willebrand disease in Oman
2024-5-13
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